rs863225017
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(-;-) | 0 | common in clinvar |
Make rs863225017(-;A) |
Make rs863225017(A;A) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | X |
Position | 31209509 |
Gene | DMD |
is a | snp |
is | mentioned by |
dbSNP | rs863225017 |
dbSNP (classic) | rs863225017 |
ClinGen | rs863225017 |
ebi | rs863225017 |
HLI | rs863225017 |
Exac | rs863225017 |
Gnomad | rs863225017 |
Varsome | rs863225017 |
LitVar | rs863225017 |
Map | rs863225017 |
PheGenI | rs863225017 |
Biobank | rs863225017 |
1000 genomes | rs863225017 |
hgdp | rs863225017 |
ensembl | rs863225017 |
geneview | rs863225017 |
scholar | rs863225017 |
rs863225017 | |
pharmgkb | rs863225017 |
gwascentral | rs863225017 |
openSNP | rs863225017 |
23andMe | rs863225017 |
SNPshot | rs863225017 |
SNPdbe | rs863225017 |
MSV3d | rs863225017 |
GWAS Ctlg | rs863225017 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs863225017(A;A) |
Alt | rs863225017(A;A) |
Reference | Rs863225017(-;-) |
Significance | Pathogenic |
Disease | Duchenne muscular dystrophy |
Variation | info |
Gene | DMD |
CLNDBN | Duchenne muscular dystrophy |
Reversed | 1 |
HGVS | NC_000023.10:g.31227627dupT |
CLNSRC | Quest Diagnostics |
CLNACC | RCV000201051.1, |